Medtronic recalls specific lots of Perfusion Systems due to potential insufficient or incomplete welds. Affected units may have safety risks requiring immediate action.
Specific lots may have been manufactured with insufficient or incomplete welds.
Medtronic is recalling certain lots of Perfusion Systems because some units might have been made with insufficient or incomplete welds. This could lead to safety issues if the device fails during use.
Insufficient or incomplete welds in the device could cause it to fail during use, potentially leading to safety risks. The exact mechanism of failure is not specified in the recall notice.
Patients using the Medtronic Perfusion System with specific lot numbers are affected. Those who have the device and are using it for medical purposes are most at risk.
Check the lot number on your device, which is listed as 221196141 for the recalled units. The product was sold with a use-by date of August 19, 2022.
Look for the lot number 221196141 on your Medtronic Perfusion System.
The recalled lot number is 221196141.
The product was sold with a use-by date of August 19, 2022.
The recall notice does not specify a remedy.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1880-2021 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1880-2021 from Medtronic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
